NDC 54868-6044
Jolessa 0.03 mg / 0.15 mg kit
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0555-9123.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.
Recalls
- Mar 15, 2013 · Class III · Teva Pharmaceuticals USA, Inc.
Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Benzene Sulfonamide (NBBS) was detected during impurity testing
Lots: NDC 0555-9123-66, Lot numbers 33802986A, exp 9/2013; 33802991A, exp 7/2013; and 33803270A, exp 10/2013. - Mar 12, 2013 · Class III · Teva Pharmaceuticals USA, Inc.
Failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.
Lots: Lot #: 33803603A, 33803604A, Exp 11/13; 33803996A, and 33803997A, Exp 03/14 - Apr 23, 2012 · Class III · Teva Pharmaceuticals USA, Inc.
Contraceptive Tablets Out of Sequence: This recall has been initiated due to the potential that some regimen packages may not contain placebo tablets.
Lots: Lot #'s 33801826A, Exp 1/2013; 33802144A; 33802323A, Exp 3/2013; 33802519A, Exp 6/2013
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ethinyl Estradiol and Levonorgestrel: every company that makes it
- Form
- kit
- Strength
- 0.03 mg / 0.15 mg
- Approval
- NDA NDA021544
- On the market since
- Jun 24, 2009
- Package NDCs
54868-6044-0- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2011
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